2-bromo-5-methoxypyridine-3-carbaldehyde

≥95%

Reagent Code: #143846
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CAS Number 1289177-58-7

science Other reagents with same CAS 1289177-58-7

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Weight 216.03 g/mol
Formula C₇H₆BrNO₂
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MDL Number MFCD26520554
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of agrochemicals and functional materials where pyridine-based scaffolds are required. Its aldehyde group enables further derivatization, including conversion to alcohols, acids, or imines, expanding its utility in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿29,850.00
inventory 500mg
10-20 days ฿103,000.00

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2-bromo-5-methoxypyridine-3-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of agrochemicals and functional materia

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of agrochemicals and functional materials where pyridine-based scaffolds are required. Its aldehyde group enables further derivatization, including conversion to alcohols, acids, or imines, expanding its utility in synthetic pathways.

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